Key result
Oral amitriptyline in horses yields an elimination half-life of ~17 hours.
Why the study?
The pharmacokinetics of oral amitriptyline in horses were not well characterized.
Answers are grounded in this paper and cite their sources.
May guide initial dosing in horses; leaves open confirmation of efficacy and safety in clinical use.
The purpose of this study was to evaluate the pharmacokinetics of oral amitriptyline in horses. Oral amitriptyline (1 mg/kg) was administered to six horses. Blood samples were collected from jugular and lateral thoracic vein at predetermined times from 0 to 24 hr after administration. Plasma concentrations were determined by high‐performance liquid chromatography and analyzed using noncompartmental methods. Pharmacodynamic parameters including heart rate, respiration rate, and intestinal motility were evaluated, and electrocardiographic examinations were performed in all subjects. The mean maximum plasma concentration (Cmax) of amitriptyline was 30.7 ng/ml, time to maximum plasma concentration (Tmax) 1–2 hr, elimination half‐life (t1/2) 17.2 hr, area under plasma concentration–time curve (AUC) 487.4 ng ml−1 hr−1, apparent clearance (Cl/F) 2.6 L hr−1 kg−1, and apparent volume of distribution (Vd/F) 60.1 L/kg. Jugular vein sampling overestimated the amount of amitriptyline absorbed and should not be used to study uptake following oral administration. Heart rate and intestinal motility showed significant variation (p < .05). Electrocardiography did not provide conclusive results. Further studies are required to discern if multiple dose treatment would take the drug to steady state as expected, consequently increasing plasma concentrations.
No takes yet. Share an insight, caveat, or question.
Recchi et al. (2020) studied this question. Oral amitriptyline was evaluated on Pharmacokinetic parameters (Cmax, Tmax, t1/2, AUC, Cl/F, Vd/F). Oral amitriptyline (1 mg/kg) in horses yielded a mean maximum plasma concentration of 30.7 ng/ml, time to maximum concentration of 1-2 hours, and elimination half-life of 17.2 hours.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: